Kyutec KT1053 Guia De Inicio Rapido página 61

This product meets the regulations of Directive 93/42 EEC
in medical device
Labeling & Information
EU Representative
This product meets the regulations of Directive 93/42 EEC
Manufactured by in medical device
Manufacture Date EU Representative
Attention, see instructions Manufactured by
Dispose of the device in accordance with the directive Manufacture Date
2002/96/EC – WEEE (Waste Electrical and Electronic Equipment)
Attention, see instructions
Application part type BF
Dispose of the device in accordance with the directive
2002/96/EC – WEEE (Waste Electrical and Electronic Equipment)
Application part type BF
HIVOX BIOTEK B.V
De Run 4428, 5503 LR
Veldhoven, Netherlands
HIVOX BIOTEK INC.
5F, No.123, Shingde Rd.,
Sanchong District 241, New Taipei City, Taiwan R.O.C
HIVOX BIOTEK B.V
De Run 4428, 5503 LR
Veldhoven, Netherlands
HIVOX BIOTEK INC.
5F, No.123, Shingde Rd.,